K-number	K080502
Device name	MODIFICATION TO:PILOT SPINAL SYSTEM
Applicant	Life Spine
Product code	MNI
Device class	Class II
Decision date	Apr 8, 2008
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO:PILOT SPINAL SYSTEM

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